Primary desmoplastic small round cell tumor of the kidney:: A case report in a 14-year-old girl with molecular confirmation

被引:11
|
作者
Collardeau-Frachon, Sophie [1 ]
Ranchere-Vince, Dominique
Delattre, Olivier
Hoarau, Stelly
Thiesse, Philippe
Dubois, Remi
Bergeron, Christophe
Dijoud, Frederique
Bouvier, Raymonde
机构
[1] Hop Edouard Herriot, Serv Anat Pathol, Lyon, France
[2] Ctr Leon Berard, Serv Anat Pathol, F-69373 Lyon, France
[3] Inst Curie, Unit Genet Somatique, Paris, France
[4] Hop Edouard Herriot, Serv Chirurg Pediat, Lyon, France
[5] Ctr Leon Berard, Serv Oncol Pediat, F-69373 Lyon, France
[6] Hop Debrousse, Serv Anat Pathol, Lyon, France
关键词
desmoplastic small round cell tumor; EWS-WT1 fusion transcript; immunophenotype; kidney; EXPRESSION; WT1;
D O I
10.2350/06-10-0177.1
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We report a case of desmoplastic small round cell tumor (DSRCT) arising in the kidney of a 14-year-old female. The subject presented with gross hematuria. Medical imaging uncovered a left renal mass without regional or metastatic extension. The tumor showed morphological, immunohistochemical, and molecular features of DSRCT. Immumostaining revealed polyphenotypic differentiation. Molecular analysis detected the fusion transcript resulting from the t(11;22)(p13;q12) reciprocal translocation, which characterized this neoplasm. Desmoplastic small round cell tumor is a rare, aggressive neoplasm that mainly affects young males and that usually presents with widespread abdominal serosal involvement. This unusual localization should lead one to consider this tumor in the differential diagnosis of small blue round cell tumors of the kidney.
引用
收藏
页码:320 / 324
页数:5
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